Tendersant Hand Sanitizer

Manufacturer: Geri-Gentle Corporation
Effective date: 2025-09-23
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-06-01 01:14:36

Label at a glance#

ProductTendersant Hand Sanitizer

Active ingredientALCOHOL

Label structure9 sections

Indications and uses

To decrease bacteria on the skin. Recommended for repeated use.

Dosage and administration

Not recommended for infants Wet hands thoroughly with product and allow to dry without wiping Children under 6 years of age should be supervised when using this product.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses:

INDICATIONS & USAGE SECTION

To decrease bacteria on the skin.

Recommended for repeated use.

Warnings

WARNINGS SECTION

Keep away from fire or flame. Flammable.

Avoid contact with broken skin. For external use only.

When using this product

OTC - WHEN USING SECTION

do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water

Stop use:

OTC - STOP USE SECTION

if irritation or redness develops.

If condition persists for more than 72 hours consult a doctor.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help

Directions:

DOSAGE & ADMINISTRATION SECTION

Not recommended for infants

Wet hands thoroughly with product and allow to dry without wiping
Children under 6 years of age should be supervised when using this product.

Other information:

SPL UNCLASSIFIED SECTION

Do not store above 110°F,

May discolor some fabrics..

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Water, Aloe Barbadensis Leaf Juice, Maltodextrin, Glycerin, Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate crosspolymer, Triethanolamine, Fragrance.

Package Labeling:118ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label

Package Labeling:500ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label

Package Labeling:236ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581662	ethanol 70 % Topical Gel	PSN	3
581662	ethanol 0.7 ML/ML Topical Gel	SCD	3
581662	ethanol 70 % Topical Gel	SY	3
581662	ethyl alcohol 70 % Topical Gel	SY	3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
69771-007-01	Tendersant Hand Sanitizer	118 mL in 1 BOTTLE	GEL	118	3
69771-007-02	Tendersant Hand Sanitizer	500 mL in 1 BOTTLE	GEL	500	3
69771-007-03	Tendersant Hand Sanitizer	236 mL in 1 BOTTLE	GEL	236	3

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 9 matching rows.

Tendersant Hand Sanitizer
ALCOHOL
WATER
ALOE VERA LEAF
MALTODEXTRIN
GLYCERIN
PROPYLENE GLYCOL
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)
TROLAMINE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
69771-007	69771-007-01, 69771-007-02, 69771-007-03

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
MALTODEXTRIN	7CVR7L4A2D	IACT
GLYCERIN	PDC6A3C0OX	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)	59TL3WG5CO	IACT
TROLAMINE	9O3K93S3TK	IACT
ALCOHOL	3K9958V90M	ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Tendersant Hand Sanitizer	ALCOHOL	Geri-Gentle Corporation	b09d568a-4c9d-5804-e053-2a95a90ab8ea	2025-09-23	Warnings	Exact identifier ndc (package): 69771-007-02 ndc (package): 69771-007-01 ndc (package): 69771-007-03 ndc (product): 69771-007 ndc11 (package): 69771000702 ndc11 (package): 69771000703 ndc11 (package): 69771000701 spl id: 3f7b3095-d1c2-4f15-e063-6394a90a50aa spl set id: b09d568a-4c9d-5804-e053-2a95a90ab8ea

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.